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Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 1/2015, Volume 38, Issue 1, pp. 123 - 136
Journal Article
Zhonghua er ke za zhi = Chinese journal of pediatrics, ISSN 0578-1310, 09/2017, Volume 55, Issue 9, p. 678
To explore the phenotypic and genotypic characteristics in Chinese children with classic pantothenate kinase-associated neurodegeneration (PKAN). The clinical,... 
Pantothenate Kinase-Associated Neurodegeneration - complications | Pantothenate Kinase-Associated Neurodegeneration - diagnosis | Brain | Pantothenate Kinase-Associated Neurodegeneration - genetics | Humans | Age of Onset | Child, Preschool | Genotype | Retrospective Studies | Dystonia - etiology | Child | Disease Progression
Journal Article
東京女子医科大学雑誌, ISSN 0040-9022, 01/2013, Volume 83, pp. E69 - E73
Pantothenate kinase-associated... 
Journal Article
Zhonghua yi xue za zhi, ISSN 0376-2491, 12/2009, Volume 89, Issue 47, p. 3320
To investigate the clinical features and detection of pantothenate kinase 2 (PANK2) gene mutation in a Chinese patient with Hallervorden-Spatz syndrome (HSS).... 
Pantothenate Kinase-Associated Neurodegeneration - diagnosis | Phenotype | Pantothenate Kinase-Associated Neurodegeneration - genetics | Pedigree | Humans | Asian Continental Ancestry Group - genetics | Adult | Female | Phosphotransferases (Alcohol Group Acceptor) - genetics | Mutation
Journal Article
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 06/2008, Volume 60, Issue 6, p. 635
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 04/2005, Volume 22, Issue 2, p. 189
To study pantothenate kinase 2 (PANK2) gene mutations in Chinese patients with Hallervorden-Spatz syndrome (HSS). PANK2 gene mutations were detected by PCR,... 
Humans | Middle Aged | Male | Phosphotransferases (Alcohol Group Acceptor) - genetics | Polymorphism, Single-Stranded Conformational | Young Adult | DNA Mutational Analysis | Pantothenate Kinase-Associated Neurodegeneration - genetics | Pedigree | Base Sequence | China | Adolescent | Polymerase Chain Reaction | Adult | Female | Mutation | Child
Journal Article
by Ohno, M and Goto, I
Nihon rinsho. Japanese journal of clinical medicine, ISSN 0047-1852, 11/1993, Volume 51, Issue 11, p. 2957
Hallervorden-Spatz disease is an autosomal recessive disorder which usually begins in childhood, progresses irreversibly and leads to death in early adulthood.... 
Prognosis | Substantia Nigra - pathology | Pantothenate Kinase-Associated Neurodegeneration - genetics | Humans | Genes, Recessive | Globus Pallidus - pathology | Pantothenate Kinase-Associated Neurodegeneration - pathology
Journal Article
Shinkei kenkyu no shimpo. Advances in neurological sciences, ISSN 0001-8724, 12/1966, Volume 10, Issue 4, p. 700
Journal Article
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